Term Name:	primary autosomal recessive microcephaly 9
Synonyms:	MCPH9
Definition:	A primary autosomal recessive microcephaly that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21.
Ontology:	Human Disease [DOID:0070292]   ( DOID:0070292 )